NEAL WRIST CONES— 510(k) K925924

Substantially Equivalent

Neal & Assoc., Inc.

FDA 510(k) clearance K925924 for NEAL WRIST CONES, Substantially Equivalent on 1993-04-08. Applicant: Neal & Assoc., Inc..

Clearance details

Applicant: Neal & Assoc., Inc.
Product code: Code FMQ
Advisory panel: General Hospital
Date received: 1992-11-23
Decision date: 1993-04-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia, MO, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code FMQ

product code FMQ

Death: 8
Total: 8

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.